Cosner J C, Troxler R F
Biochim Biophys Acta. 1978 Jul 24;519(2):474-88. doi: 10.1016/0005-2787(78)90100-4.
Stable and metabolically active protoplasts were prepared from the unicellular cyanophyte, Anacystis nidulans, by enzymatic digestion of the cell wall with 0.1% lysozyme. The yield of protoplasts from intact algal cells was approx. 50%. Incorporation of L-[U-14C]leucine into cold trichloroacetic acid-insoluble material from protoplasts preparations was linear for 1.5 h and continued for an additional 2.5 h. Incorporation of radiolabeled leucine into hot trichloroacetic acid-insoluble material from protoplast preparations demonstrated protein synthesis in protoplasts in vitro. Phycocyanin is the principal phycobiliprotein and allophycocyanin is a minor phycobiliprotein in A. nidulans cells. The light-absorbing chromophore of both of these phycobiliproteins is the linear tetrapyrrole (bile pigment), phycocyanobilin. Radiolabeled phycocyanin and allophycocyanin were isolated from protoplast preparations which had been incubated with L-[U-14]leucine or delta-amino[4-14C] levulinic acid (a precursor of phycocyanobilin). The radio-labeled phycobiliproteins were purified by ammonium sulfate fractionation and ion-exchange chromatography on brushite columns. The specific radioactivity of phycocyanin and allophycocyanin in brushite column eluates (protoplasts incubated with radiolabeled leucine) was 106 000 and 82 000 dpm/mg, respectively. The specific radioactivity of phycocyanin and allophycocyanin in brushite column eluates (protoplasts incubated with radiolabeled delta-aminolevulinic acid) was 33 000 and 38 000 dpm/mg, respectively. Phycobiliproteins from protoplasts incubated with radiolabeled leucine were examined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. 25% of the incorporated radioactivity in protoplast lysates and approx. 60% of the incorporated radioactivity in protoplast lysates and approx. 60% of the incorporated ratioactivity in phycocyanin and allophycocyanin (in brushite column eluates) comigrated with the subunits of these phycobiliproteins on sodium dodecyl sulfate-polyacrylamide gels. Chromic acid degradation of phycobiliproteins from protoplast preparations incubated with delta-amino[4-14C] levulinic acid yielded radiolabeled imides which were derived from the phycocyanobilin chromophore. Imides from radiolabeled phycobiliproteins isolated from protoplast preparations incubated with L-[U-14C]leucine did not contain radioactivity. These results show that both the apoprotein and tetrapyrrolic moieties of phycocyanin and allophycocyanin were synthesized in A. nidulans protoplasts in vitro.
通过用0.1%溶菌酶酶解细胞壁,从单细胞蓝藻集胞藻中制备出稳定且代谢活跃的原生质体。完整藻细胞的原生质体产量约为50%。原生质体制备物中L-[U-¹⁴C]亮氨酸掺入冷的三氯乙酸不溶性物质的过程在1.5小时内呈线性,并持续另外2.5小时。将放射性标记的亮氨酸掺入原生质体制备物的热的三氯乙酸不溶性物质中,证明了原生质体在体外的蛋白质合成。藻蓝蛋白是集胞藻细胞中的主要藻胆蛋白,别藻蓝蛋白是次要藻胆蛋白。这两种藻胆蛋白的吸光发色团都是线性四吡咯(胆色素),即藻蓝胆素。从用L-[U-¹⁴]亮氨酸或δ-氨基[4-¹⁴C]乙酰丙酸(藻蓝胆素的前体)孵育的原生质体制备物中分离出放射性标记的藻蓝蛋白和别藻蓝蛋白。放射性标记的藻胆蛋白通过硫酸铵分级分离和在透钙磷石柱上的离子交换色谱法进行纯化。透钙磷石柱洗脱液(用放射性标记的亮氨酸孵育的原生质体)中藻蓝蛋白和别藻蓝蛋白的比放射性分别为106000和82000 dpm/mg。透钙磷石柱洗脱液(用放射性标记的δ-氨基乙酰丙酸孵育的原生质体)中藻蓝蛋白和别藻蓝蛋白的比放射性分别为33000和38000 dpm/mg。用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳检查用放射性标记的亮氨酸孵育的原生质体中的藻胆蛋白。原生质体裂解物中25%的掺入放射性以及藻蓝蛋白和别藻蓝蛋白(在透钙磷石柱洗脱液中)中约60%的掺入放射性与这些藻胆蛋白的亚基在十二烷基硫酸钠-聚丙烯酰胺凝胶上共迁移。用δ-氨基[4-¹⁴C]乙酰丙酸孵育的原生质体制备物中的藻胆蛋白经铬酸降解产生了源自藻蓝胆素发色团的放射性标记的酰亚胺。从用L-[U-¹⁴C]亮氨酸孵育的原生质体制备物中分离出的放射性标记藻胆蛋白的酰亚胺不含放射性。这些结果表明,藻蓝蛋白和别藻蓝蛋白的脱辅基蛋白和四吡咯部分都是在集胞藻原生质体中体外合成的。